Based on the pET-28a map and based on the nucleotide sequence of the OXA-M290 gene, could the restriction enzymes SacI and HindIII be used when cloning the OXA-M290 gene into pET-28a? Why or why not?

Human Anatomy & Physiology (11th Edition)
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ISBN:9780134580999
Author:Elaine N. Marieb, Katja N. Hoehn
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For this biology course and based on the results obtained from a previous BLAST search, the bacteria responsible for the infection at a Hospital is most likely a new strain of Escherichia coli. This strain is given the name E. coli AFB. 

Earlier, BLAST was used to study a resistance gene from E. coli AFB. These analyses suggest that this strain produces a new β-lactamase, which is given the name OXA-M290. Also, primers were designed to amplify the gene encoding OXA-M290 by PCR. 

The next step is to clone the PCR-amplified OXA-M290 gene into an expression vector, so that recombinant OXA-M290 protein can be produced and studied. You will start by going over the process of cloning the OXA-M290 gene into pET-28a. Be sure to reference a plasmid map for pET-28a.

Here is the nucleotide sequence for the OXA-M290 gene:

>OXA-M290 
ATGCGTGTATTAGCCTTATCGGCTGTGTTTTTGGTGGCATCGATT 
ATCGGAATGCCTGCGGTAGCAAAGGAATGGCAAGAAAACAAAAGT 
TGGAATGCTCACTTTACTGAACATAAATCACAGGGCGTAGTTGTG 
CTCTGGAATGAGAATAAGCAGCAAGGATTTACCAATAATCTTAAA 
CGGGCGAACCAAGCATTTTTACCCGCATCTAGTGCGAAAATTCCC 
AATAGCTTGATCGCCCTCGATTTGGGCGTGGTTAAGGATGAACAC 
CAAGTCTTTAAGTGGGATGGACAGACGCGCGATATCGCCACTTGG 
AATCGCGATCATAATCTAATCACCGCGATGAAATATTCAGTTGTG 
CCTGTTTATCAAGAATTTGCCCGCCAAATTGGCGAGGCACGTATG 
AGCAAGATGCTACATGCTTTCGATTATGGTAATGAGGACATTTCG 
GGCAATGTAGACAGTTTCTGGCTCGACGGTGGTATTCGAATTTCG 
GCCACGGAGCAAATCAGCTTTTTAAGAAAGCTGTATCACAATAAG 
TTACACGTATCGGAGCGCAGCCAGCGTATTGTCAAACAAGCCATG 
CTGACCGAAGCCAATGGCGACTATATTATTCGGGCTAAAACTGGA 
TACGATACTAAGATTGGCTGGTGGGTCGGTTGGGTTGAACTTGAT 
GATAATGTGTGGTTTTTTGCGATGAATATGGATATGCCCACATCG 
GATGGTTTAGGGCTGCGCCAAGCCATCACAAAAGAAGTGCTCAAA 
CAGGAAAAAATTATTCCCTAG 

Based on the pET-28a map and based on the nucleotide sequence of the OXA-M290 gene, could the restriction enzymes SacI and HindIII be used when cloning the OXA-M290 gene into pET-28a? Why or why not? A free tool called NEBcutter ( https://nc3.neb.com/NEBcutter/ ) might be useful for answering this question. [3 – 4 sentences suggested] 

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